Study on application of multiplex ligation-dependent probe amplification (MLPA) assay in molecular diagnosis of retinoblastoma /

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Study on application of multiplex ligation-dependent probe amplification (MLPA) assay in molecular diagnosis of retinoblastoma /

محفوظ في:

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Vu Phuong Nhung.
مؤلفون آخرون:	Ma Thi Huyen Thuong., Nguyen Dang Ton., Nguyen Hai Ha., Nguyen Thi Thanh Hoa., Nguyen Thuy Duong., Nong Van Hai., Tran Thi Bich Ngoc.
التنسيق:	مقال
اللغة:	Vietnamese
الموضوعات:	Deletions Duplications mutation Genetic counseling MLPA RB1 gene Retinoblastoma
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

Thư viện lưu trữ:	Thư viện Trường Đại học Đà Lạt

مواد مشابهة

Ứng dụng kỹ thuật Multiplex Ligation-Dependent Probe Amplification (MLPA) khảo sát nhóm gen gây bệnh thần kinh di truyền Charcot-Marie-Tooth
بواسطة: Nguyễn, Nhật Quỳnh Như, وآخرون
منشور في: (2023)

Ứng dụng kỹ thuật Multiplex Ligation-Dependent Probe Amplification (MLPA) khảo sát nhóm gen gây bệnh thần kinh di truyền C-harcot-Marie-Tooth
بواسطة: Nguyễn, Nhật Quỳnh Như, وآخرون
منشور في: (2025)

Xác định đột biến gen α-thalassemia bằng kỹ thuật Multiplex ligation-dependent probe amplification
بواسطة: Lê, Thị Phương, وآخرون
منشور في: (2025)

G2-phase chromosomal radiosensitivity of primary fibroblasts from hereditary retinoblastoma family members and some apparently normal controls /

Ứng dụng kỹ thuật Multiplex ligation – dependent probe amplification (MLPA) khảo sát đột biến mất đoạn gen CYP21A2 gây bệnh tăng sản thượng thận bẩm sinh
بواسطة: Nguyễn, Nhật Quỳnh Như, وآخرون
منشور في: (2024)

Ứng dụng kỹ thuật Multiplex ligation-dependent probe amplification xác định người lành mang đột biến gen α-thalassemia
بواسطة: Nguyễn, Minh Ngọc, وآخرون
منشور في: (2023)

Ứng dụng kỹ thuật Multiplex ligation-dependent probe amplification xác định người lành mang đột biến gen α-thalassemia
بواسطة: Nguyễn, Minh Ngọc, وآخرون
منشور في: (2025)

Ứng dụng kỹ thuật multiplex ligation-dependent probe amplification xác định đột biến gen α thalassemia ở bệnh nhân HbH
بواسطة: Lê, Thanh Hằng, وآخرون
منشور في: (2023)

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